Linked Data
ClinVar Variation Id:
2953230
ClinVar RCV Id:
RCV003810348
MyVariant Identifiers:
chr1:g.68896989G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68431306G>T , CM000663.2:g.68431306G>T | GRCh38 |
| NC_000001.10:g.68896989G>T , CM000663.1:g.68896989G>T | GRCh37 |
| NC_000001.9:g.68669577G>T | NCBI36 |
| NG_008472.1:g.23654C>A | |
| NG_008472.2:g.23654C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1314C>A MANE Select | ENSP00000262340.5:p.Gly438= | |
| ENST00000262340.5:c.1314C>A | ENSP00000262340.5:p.Gly438= | |
| NM_000329.2:c.1314C>A | NP_000320.1:p.Gly438= | |
| XM_017002027.1:c.1038C>A | XP_016857516.1:p.Gly346= | |
| NM_000329.3:c.1314C>A MANE Select | NP_000320.1:p.Gly438= |